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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1952 1
1985 2
1988 1
1992 2
1993 3
1994 2
1995 1
1996 3
1997 1
1998 2
1999 1
2000 5
2001 7
2002 3
2003 7
2004 7
2005 8
2006 10
2007 9
2008 8
2009 4
2010 3
2011 4
2012 1
2015 1
2024 0

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89 results

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Page 1
Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome.
Bonadona V, Bonaïti B, Olschwang S, Grandjouan S, Huiart L, Longy M, Guimbaud R, Buecher B, Bignon YJ, Caron O, Colas C, Noguès C, Lejeune-Dumoulin S, Olivier-Faivre L, Polycarpe-Osaer F, Nguyen TD, Desseigne F, Saurin JC, Berthet P, Leroux D, Duffour J, Manouvrier S, Frébourg T, Sobol H, Lasset C, Bonaïti-Pellié C; French Cancer Genetics Network. Bonadona V, et al. JAMA. 2011 Jun 8;305(22):2304-10. doi: 10.1001/jama.2011.743. JAMA. 2011. PMID: 21642682
[Oncogenetic consultation for breast cancer].
Chompret A, Noguès C, Stoppa-Lyonnet D. Chompret A, et al. Presse Med. 2007 Feb;36(2 Pt 2):357-63. doi: 10.1016/j.lpm.2006.12.003. Epub 2007 Jan 9. Presse Med. 2007. PMID: 17258685 Review. French.
Molecular basis of the Li-Fraumeni syndrome: an update from the French LFS families.
Bougeard G, Sesboüé R, Baert-Desurmont S, Vasseur S, Martin C, Tinat J, Brugières L, Chompret A, de Paillerets BB, Stoppa-Lyonnet D, Bonaïti-Pellié C, Frébourg T; French LFS working group. Bougeard G, et al. Among authors: chompret a. J Med Genet. 2008 Aug;45(8):535-8. doi: 10.1136/jmg.2008.057570. Epub 2008 May 29. J Med Genet. 2008. PMID: 18511570
BRAF as a melanoma susceptibility candidate gene?
Laud K, Kannengiesser C, Avril MF, Chompret A, Stoppa-Lyonnet D, Desjardins L, Eychene A, Demenais F, Lenoir GM, Bressac-de Paillerets B; French Herediatary Melanoma Study Group. Laud K, et al. Among authors: chompret a. Cancer Res. 2003 Jun 15;63(12):3061-5. Cancer Res. 2003. PMID: 12810628
A single Mediterranean, possibly Jewish, origin for the Val59Gly CDKN2A mutation in four melanoma-prone families.
Yakobson E, Eisenberg S, Isacson R, Halle D, Levy-Lahad E, Catane R, Safro M, Sobolev V, Huot T, Peters G, Ruiz A, Malvehy J, Puig S, Chompret A, Avril MF, Shafir R, Peretz H, Bressac-de Paillerets B. Yakobson E, et al. Among authors: chompret a. Eur J Hum Genet. 2003 Apr;11(4):288-96. doi: 10.1038/sj.ejhg.5200961. Eur J Hum Genet. 2003. PMID: 12700603
A 22-year French experience with solid tumors in children with Down syndrome.
Satgé D, Sasco AJ, Chompret A, Orbach D, Méchinaud F, Lacour B, Roullet B, Martelli H, Bergeron C, Bertrand Y, Lacombe D, Perel Y, Monteil P, Nelken B, Bertozzi AI, Munzer M, Kanold J, Bernard F, Vekemans MJ, Sommelet D. Satgé D, et al. Among authors: chompret a. Pediatr Hematol Oncol. 2003 Oct-Nov;20(7):517-29. doi: 10.1080/08880010390232727. Pediatr Hematol Oncol. 2003. PMID: 12959856
[Li-Fraumeni syndrome: update, new data and guidelines for clinical management].
Frebourg T, Abel A, Bonaiti-Pellie C, Brugières L, Berthet P, Bressac-de Paillerets B, Chevrier A, Chompret A, Cohen-Haguenauer O, Delattre O, Feingold J, Feunteun J, Frappaz D, Fricker JP, Gesta P, Jonveaux P, Kalifa C, Lasset C, Leheup B, Limacher JM, Longy M, Nogues C, Oppenheim D, Sommelet D, Soubrier F, Stoll C, Stoppa-Lyonnet D, Tristant H. Frebourg T, et al. Among authors: chompret a. Bull Cancer. 2001 Jun;88(6):581-7. Bull Cancer. 2001. PMID: 11459705 Free article. Review. French.
A single genetic origin for the G101W CDKN2A mutation in 20 melanoma-prone families.
Ciotti P, Struewing JP, Mantelli M, Chompret A, Avril MF, Santi PL, Tucker MA, Bianchi-Scarrà G, Bressac-de Paillerets B, Goldstein AM. Ciotti P, et al. Among authors: chompret a. Am J Hum Genet. 2000 Aug;67(2):311-9. doi: 10.1086/303001. Epub 2000 Jun 22. Am J Hum Genet. 2000. PMID: 10869234 Free PMC article.
89 results